PMID- 22963517 OWN - NLM STAT- MEDLINE DCOM- 20121218 LR - 20240117 IS - 1532-429X (Electronic) IS - 1097-6647 (Print) IS - 1097-6647 (Linking) VI - 14 IP - 1 DP - 2012 Sep 10 TI - Extracellular volume fraction mapping in the myocardium, part 1: evaluation of an automated method. PG - 63 LID - 10.1186/1532-429X-14-63 [doi] AB - BACKGROUND: Disturbances in the myocardial extracellular volume fraction (ECV), such as diffuse or focal myocardial fibrosis or edema, are hallmarks of heart disease. Diffuse ECV changes are difficult to assess or quantify with cardiovascular magnetic resonance (CMR) using conventional late gadolinium enhancement (LGE), or pre- or post-contrast T1-mapping alone. ECV measurement circumvents factors that confound T1-weighted images or T1-maps, and has been shown to correlate well with diffuse myocardial fibrosis. The goal of this study was to develop and evaluate an automated method for producing a pixel-wise map of ECV that would be adequately robust for clinical work flow. METHODS: ECV maps were automatically generated from T1-maps acquired pre- and post-contrast calibrated by blood hematocrit. The algorithm incorporates correction of respiratory motion that occurs due to insufficient breath-holding and due to misregistration between breath-holds, as well as automated identification of the blood pool. Images were visually scored on a 5-point scale from non-diagnostic (1) to excellent (5). RESULTS: The quality score of ECV maps was 4.23 +/- 0.83 (m +/- SD), scored for n=600 maps from 338 patients with 83% either excellent or good. Co-registration of the pre-and post-contrast images improved the image quality for ECV maps in 81% of the cases. ECV of normal myocardium was 25.4 +/- 2.5% (m +/- SD) using motion correction and co-registration values and was 31.5 +/- 8.7% without motion correction and co-registration. CONCLUSIONS: Fully automated motion correction and co-registration of breath-holds significantly improve the quality of ECV maps, thus making the generation of ECV-maps feasible for clinical work flow. FAU - Kellman, Peter AU - Kellman P AD - National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD, USA. kellmanp@nhlbi.nih.gov FAU - Wilson, Joel R AU - Wilson JR FAU - Xue, Hui AU - Xue H FAU - Ugander, Martin AU - Ugander M FAU - Arai, Andrew E AU - Arai AE LA - eng GR - ZIA HL004607-14/ImNIH/Intramural NIH HHS/United States GR - ZID HL006140-02/ImNIH/Intramural NIH HHS/United States GR - ZID HL006140-01/ImNIH/Intramural NIH HHS/United States GR - ZIE HL006139-02/ImNIH/Intramural NIH HHS/United States GR - ZIE HL006139-01/ImNIH/Intramural NIH HHS/United States PT - Comparative Study PT - Journal Article DEP - 20120910 PL - England TA - J Cardiovasc Magn Reson JT - Journal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance JID - 9815616 SB - IM MH - Aged MH - *Algorithms MH - Cardiomyopathies/*pathology MH - Female MH - Fibrosis MH - Follow-Up Studies MH - Humans MH - Image Enhancement/*methods MH - Magnetic Resonance Imaging, Cine/*methods MH - Male MH - Middle Aged MH - Myocardium/*pathology MH - Retrospective Studies PMC - PMC3441905 EDAT- 2012/09/12 06:00 MHDA- 2012/12/19 06:00 PMCR- 2012/09/10 CRDT- 2012/09/12 06:00 PHST- 2012/05/02 00:00 [received] PHST- 2012/09/03 00:00 [accepted] PHST- 2012/09/12 06:00 [entrez] PHST- 2012/09/12 06:00 [pubmed] PHST- 2012/12/19 06:00 [medline] PHST- 2012/09/10 00:00 [pmc-release] AID - S1097-6647(23)00686-5 [pii] AID - 1532-429X-14-63 [pii] AID - 10.1186/1532-429X-14-63 [doi] PST - epublish SO - J Cardiovasc Magn Reson. 2012 Sep 10;14(1):63. doi: 10.1186/1532-429X-14-63.